Drug recall
Panacea Air Pro Mattress Control Unit, Model: Platinum 5000, US Model Number 5000. Use with alternating…
FDA recall event 74737 · Class II · American National Mfg Inc
Key facts
| Event ID | 74737 |
|---|---|
| Recall numbers | Z-2605-2016 |
| Recalling firm | American National Mfg Inc |
| Product type | Devices |
| Products | Panacea Air Pro Mattress Control Unit, Model: Platinum 5000, US Model Number 5000. Use with alternating pressure air flotation mattress. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The Panacea Air Pro Mattress Control Unit is being recalled due to a firmware problem, which may result in the device not having the firmness range required. |
| Initiation date | Jul 11, 2016 |
| Report date | Aug 31, 2016 |
| Termination date | Jan 17, 2017 |
| City | Corona |
| State | CA |
| Country | United States |
| FEI number | 3000204953 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: